Canonical Allele Identifier: CA382035411

Gene: TYR

Linked Data

• MyVariant Identifiers: chr11:g.88911889C>G (hg19) ; chr11:g.89178721C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178721C>G , CM000673.2:g.89178721C>G	GRCh38
NC_000011.9:g.88911889C>G , CM000673.1:g.88911889C>G	GRCh37
NC_000011.8:g.88551537C>G	NCBI36
NG_008748.1:g.5850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.768C>G MANE Select	ENSP00000263321.4:p.His256Gln
ENST00000263321.5:c.768C>G	ENSP00000263321.4:p.His256Gln
ENST00000526139.1:n.829C>G
NM_000372.4:c.768C>G	NP_000363.1:p.His256Gln
XM_011542970.1:c.768C>G	XP_011541272.1:p.His256Gln
XM_011542970.2:c.768C>G	XP_011541272.1:p.His256Gln
XR_001748321.1:n.2718-65188G>C
XR_001748322.1:n.2733-65188G>C
NM_000372.5:c.768C>G MANE Select	NP_000363.1:p.His256Gln